Noradrenaline and Parkinson's Disease
Identifieur interne : 000325 ( Pmc/Curation ); précédent : 000324; suivant : 000326Noradrenaline and Parkinson's Disease
Auteurs : Claire Delaville [France] ; Philippe Deurwaerdère [France] ; Abdelhamid Benazzouz [France]Source :
- Frontiers in Systems Neuroscience ; 2011.
Abstract
Parkinson's disease (PD) is characterized by the degeneration of dopamine (DA) neurons in the substantia nigra
Url:
DOI: 10.3389/fnsys.2011.00031
PubMed: 21647359
PubMed Central: 3103977
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PMC:3103977Le document en format XML
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<country>Bordeaux, France</country>
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<author><name sortKey="Deurwaerdere, Philippe De" sort="Deurwaerdere, Philippe De" uniqKey="Deurwaerdere P" first="Philippe" last="Deurwaerdère">Philippe Deurwaerdère</name>
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<author><name sortKey="Benazzouz, Abdelhamid" sort="Benazzouz, Abdelhamid" uniqKey="Benazzouz A" first="Abdelhamid" last="Benazzouz">Abdelhamid Benazzouz</name>
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<country>Bordeaux, France</country>
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<country xml:lang="fr">France</country>
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<series><title level="j">Frontiers in Systems Neuroscience</title>
<idno type="e-ISSN">1662-5137</idno>
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<front><div type="abstract" xml:lang="en"><p>Parkinson's disease (PD) is characterized by the degeneration of dopamine (DA) neurons in the substantia nigra <italic>pars compacta</italic>
, and motor symptoms including bradykinesia, rigidity, and tremor at rest. These symptoms are exhibited when striatal dopamine concentration has decreased by around 70%. In addition to motor deficits, PD is also characterized by the non-motor symptoms. However, depletion of DA alone in animal models has failed to simultaneously elicit both the motor and non-motor deficits of PD, possibly because the disease is a multi-system disorder that features a profound loss in other neurotransmitter systems. There is growing evidence that additional loss of noradrenaline (NA) neurons of the locus coeruleus, the principal source of NA in the brain, could be involved in the clinical expression of motor as well as in non-motor deficits. In the present review, we analyze the latest evidence for the implication of NA in the pathophysiology of PD obtained from animal models of parkinsonism and from parkinsonian patients. Recent studies have shown that NA depletion alone, or combined with DA depletion, results in motor as well as in non-motor dysfunctions. In addition, by using selective agonists and antagonists of noradrenaline alpha receptors we, and others, have shown that α2 receptors are implicated in the control of motor activity and that α2 receptor antagonists can improve PD motor symptoms as well as <sc>l</sc>
-Dopa-induced dyskinesia. In this review we argue that the loss of NA neurons in PD has an impact on all PD symptoms and that the addition of NAergic agents to dopaminergic medication could be beneficial in the treatment of the disease.</p>
</div>
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<pmc article-type="review-article"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Front Syst Neurosci</journal-id>
<journal-id journal-id-type="publisher-id">Front. Syst. Neurosci.</journal-id>
<journal-title-group><journal-title>Frontiers in Systems Neuroscience</journal-title>
</journal-title-group>
<issn pub-type="epub">1662-5137</issn>
<publisher><publisher-name>Frontiers Research Foundation</publisher-name>
</publisher>
</journal-meta>
<article-meta><article-id pub-id-type="pmid">21647359</article-id>
<article-id pub-id-type="pmc">3103977</article-id>
<article-id pub-id-type="doi">10.3389/fnsys.2011.00031</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Neuroscience</subject>
<subj-group><subject>Review Article</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group><article-title>Noradrenaline and Parkinson's Disease</article-title>
</title-group>
<contrib-group><contrib contrib-type="author"><name><surname>Delaville</surname>
<given-names>Claire</given-names>
</name>
<xref ref-type="aff" rid="aff1"><sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2"><sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Deurwaerdère</surname>
<given-names>Philippe De</given-names>
</name>
<xref ref-type="aff" rid="aff1"><sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2"><sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Benazzouz</surname>
<given-names>Abdelhamid</given-names>
</name>
<xref ref-type="aff" rid="aff1"><sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2"><sup>2</sup>
</xref>
<xref ref-type="aff" rid="aff3"><sup>3</sup>
</xref>
<xref ref-type="author-notes" rid="fn001">*</xref>
</contrib>
</contrib-group>
<aff id="aff1"><sup>1</sup>
<institution>UMR 5293, Institut des Maladies Neurodégénératives, Université de Bordeaux</institution>
<country>Bordeaux, France</country>
</aff>
<aff id="aff2"><sup>2</sup>
<institution>UMR 5293, Institut des Maladies Neurodégénératives, Centre National de la Recherche Scientifique</institution>
<country>Bordeaux, France</country>
</aff>
<aff id="aff3"><sup>3</sup>
<institution>Centre Hospitalier Universitaire</institution>
<country>Bordeaux, France</country>
</aff>
<author-notes><fn fn-type="edited-by"><p>Edited by: Elizabeth Abercrombie, Rutgers-Newark: The State University of New Jersey, USA</p>
</fn>
<fn fn-type="edited-by"><p>Reviewed by: Christine E. Collins, Vanderbilt University, USA; Alessandro Stefani, University of Rome, Italy</p>
</fn>
<corresp id="fn001">*Correspondence: Abdelhamid Benazzouz, Institut des Maladies Neurodégénératives, Université Bordeaux Segalen, 146, rue Léo-Saignat, 33076 Bordeaux Cedex, France. e-mail: <email>abdelhamid.benazzouz@u-bordeaux2.fr</email>
</corresp>
</author-notes>
<pub-date pub-type="epreprint"><day>27</day>
<month>3</month>
<year>2011</year>
</pub-date>
<pub-date pub-type="epub"><day>18</day>
<month>5</month>
<year>2011</year>
</pub-date>
<pub-date pub-type="collection"><year>2011</year>
</pub-date>
<volume>5</volume>
<elocation-id>31</elocation-id>
<history><date date-type="received"><day>02</day>
<month>2</month>
<year>2011</year>
</date>
<date date-type="accepted"><day>04</day>
<month>5</month>
<year>2011</year>
</date>
</history>
<permissions><copyright-statement>Copyright © 2011 Delaville, De Deurwaerdère and Benazzouz.</copyright-statement>
<copyright-year>2011</copyright-year>
<license license-type="open-access" xlink:href="http://www.frontiersin.org/licenseagreement"><license-p>This is an open-access article subject to a non-exclusive license between the authors and Frontiers Media SA, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and other Frontiers conditions are complied with.</license-p>
</license>
</permissions>
<abstract><p>Parkinson's disease (PD) is characterized by the degeneration of dopamine (DA) neurons in the substantia nigra <italic>pars compacta</italic>
, and motor symptoms including bradykinesia, rigidity, and tremor at rest. These symptoms are exhibited when striatal dopamine concentration has decreased by around 70%. In addition to motor deficits, PD is also characterized by the non-motor symptoms. However, depletion of DA alone in animal models has failed to simultaneously elicit both the motor and non-motor deficits of PD, possibly because the disease is a multi-system disorder that features a profound loss in other neurotransmitter systems. There is growing evidence that additional loss of noradrenaline (NA) neurons of the locus coeruleus, the principal source of NA in the brain, could be involved in the clinical expression of motor as well as in non-motor deficits. In the present review, we analyze the latest evidence for the implication of NA in the pathophysiology of PD obtained from animal models of parkinsonism and from parkinsonian patients. Recent studies have shown that NA depletion alone, or combined with DA depletion, results in motor as well as in non-motor dysfunctions. In addition, by using selective agonists and antagonists of noradrenaline alpha receptors we, and others, have shown that α2 receptors are implicated in the control of motor activity and that α2 receptor antagonists can improve PD motor symptoms as well as <sc>l</sc>
-Dopa-induced dyskinesia. In this review we argue that the loss of NA neurons in PD has an impact on all PD symptoms and that the addition of NAergic agents to dopaminergic medication could be beneficial in the treatment of the disease.</p>
</abstract>
<kwd-group><kwd>Parkinson's disease</kwd>
<kwd>motor and non-motor symptoms</kwd>
<kwd>noradrenaline</kwd>
<kwd>dopamine</kwd>
<kwd>locus coeruleus</kwd>
</kwd-group>
<counts><fig-count count="1"></fig-count>
<table-count count="2"></table-count>
<equation-count count="0"></equation-count>
<ref-count count="155"></ref-count>
<page-count count="12"></page-count>
<word-count count="11993"></word-count>
</counts>
</article-meta>
</front>
<body><sec sec-type=""><title>Introduction</title>
<p>Parkinson's disease (PD) is a degenerative disorder of the central nervous system that impairs motor skills, cognitive processes, and other functions. Motor symptoms are characterized by tremor, rigidity, bradykinesia, and postural instability. Among non-motor symptoms are autonomic dysfunction, sensory and sleep difficulties, cognitive, and neurobehavioral problems, including dementia and depression. For example, depression occurs in approximately 45% of all PD patients and reduces patient's quality of life independently from motor symptoms (Lemke et al., <xref ref-type="bibr" rid="B87">2004</xref>
). These non-motor symptoms are common in the advanced stages of the disease.</p>
<p>Parkinson's disease is a non-hereditary disease of unknown etiology that usually appears after the age of 50 and affects both sexes equally (Jankovic and Talosa, <xref ref-type="bibr" rid="B72">1988</xref>
). It is well-known to be characterized by a progressive degeneration of dopaminergic (DAergic) neurons (70–75%) in the substantia nigra <italic>pars compacta</italic>
(SNc), which results in a dopamine (DA) depletion in the striatum (Ehringer and Hornykiewicz, <xref ref-type="bibr" rid="B46">1960</xref>
). However, it is misleading to reduce PD to a malady of the SNc. Indeed, it has been repeatedly shown over the last 50 years that noradrenergic (NAergic) cells from the locus coeruleus (LC) also degenerate in the disease (Greenfield and Bosanquet, <xref ref-type="bibr" rid="B61">1953</xref>
; Ehringer and Hornykiewicz, <xref ref-type="bibr" rid="B46">1960</xref>
; German et al., <xref ref-type="bibr" rid="B59">1992</xref>
; Bertrand et al., <xref ref-type="bibr" rid="B20">1997</xref>
; Tohgi et al., <xref ref-type="bibr" rid="B144">1997</xref>
; Ehringer and Hornykiewicz, <xref ref-type="bibr" rid="B47">1998</xref>
). The neuronal loss in the LC is greater (83%) than in the SNc (78%; Zarow et al., <xref ref-type="bibr" rid="B155">2003</xref>
). This is in agreement with the Braak's theory (Braak and Del Tredici, <xref ref-type="bibr" rid="B23">2008</xref>
) that proposed a progressive caudo-rostral alteration of monoaminergic centers in the symptomatology of PD with a degeneration of LC NAergic neurons occurring before that of SNc DAergic neurons. Several studies revealed the existence of a correlation between the severity of DA and noradrenaline (NA) depletions with the severity of PD neurological symptoms (Marie et al., <xref ref-type="bibr" rid="B90">1995</xref>
; Selikhova et al., <xref ref-type="bibr" rid="B132">2002</xref>
). While the DAergic system is the main target of the pharmacological approaches to PD, corrections of the NA alterations inherent to the disease could improve the efficacy of current therapies. In this review we focus on the implication of the LC NA system in the pathophysiology of PD and on the different therapeutic approaches using NAergic agents.</p>
</sec>
<sec><title>Noradrenergic Systems in the Central Nervous System</title>
<sec><title>The noradrenergic system</title>
<p>Two main NAergic systems can be distinguished: one is composed of neurons belonging to the medulla oblongata (A1/C1 nucleus), whereas the other is more rostral (A2/C2 nucleus) and is located in the pons (Gaspar, <xref ref-type="bibr" rid="B57">1994</xref>
). The caudal NAergic system corresponds to diffuse groups of cells in the lower brainstem. The rostral NAergic system corresponds mainly to the locus coeruleus (LC, A6) located in the pons.</p>
<p>Noradrenaline release exerts potent neuromodulatory effects on synaptic transmission, changing the membrane potential, excitability of neurons and synaptic plasticity <italic>via</italic>
adrenergic receptors (ARs). Two subtypes of ARs have been described: alpha ARs (α1 and α2) and beta ARs (β1, β2, and β3). These ARs are found throughout the brain including the striatum and substantia nigra. Different subtypes are coupled to different G proteins. In general, excitatory effects are mediated by α1 and β postsynaptic ARs (McCormick and Wang, <xref ref-type="bibr" rid="B99">1991</xref>
; McCormick et al., <xref ref-type="bibr" rid="B98">1991</xref>
; Arcos et al., <xref ref-type="bibr" rid="B4">2003</xref>
) and inhibitory effects by α2 presynaptic ARs (Belujon et al., <xref ref-type="bibr" rid="B14">2007</xref>
; Benarroch, <xref ref-type="bibr" rid="B15">2009</xref>
; Table <xref ref-type="table" rid="T1">1</xref>
).</p>
<table-wrap id="T1" position="float"><label>Table 1</label>
<caption><p><bold>Adrenergic receptor characteristics</bold>
.</p>
</caption>
<table frame="hsides" rules="groups"><thead><tr><th align="left" rowspan="1" colspan="1">Receptor subtypes</th>
<th align="left" rowspan="1" colspan="1">G protein</th>
<th align="left" rowspan="1" colspan="1">Distribution</th>
<th align="left" rowspan="1" colspan="1">Effects</th>
</tr>
</thead>
<tbody><tr><td align="left" valign="top" rowspan="1" colspan="1">Alpha 1</td>
<td align="left" valign="top" rowspan="1" colspan="1">Gq</td>
<td align="left" valign="top" rowspan="1" colspan="1">Postsynaptic throughout brain (including cortex, thalamus, STN, Striatum…)</td>
<td align="left" valign="top" rowspan="1" colspan="1">↑ Excitability</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1">Alpha 2</td>
<td align="left" valign="top" rowspan="1" colspan="1">Gi/o</td>
<td align="left" valign="top" rowspan="1" colspan="1">Presynaptic on NAergic and non-NAergic terminals</td>
<td align="left" valign="top" rowspan="1" colspan="1">↓ Spontaneous firing and excitability;</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"></td>
<td align="left" valign="top" rowspan="1" colspan="1">↓ Neurotransmitter release</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1">Beta 1</td>
<td align="left" valign="top" rowspan="1" colspan="1">Gs</td>
<td align="left" valign="top" rowspan="1" colspan="1">Postsynaptic in cerebral cortex, mainly expressed in the heart and the kidney</td>
<td align="left" valign="top" rowspan="1" colspan="1">Adenylate cyclase activation; diffuse cellular response</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1">Beta 2</td>
<td align="left" valign="top" rowspan="1" colspan="1">Gs/Gi</td>
<td align="left" valign="top" rowspan="1" colspan="1">Postsynaptic in cerebellum and cerebral cortex, hippocampus, midbrain…, mainly expressed in peripheral nervous system</td>
<td align="left" valign="top" rowspan="1" colspan="1">Adenylate cyclase activation, resulting in an increase of cAMP; LTP facilitation</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1">Beta 3</td>
<td align="left" valign="top" rowspan="1" colspan="1">Gs</td>
<td align="left" valign="top" rowspan="1" colspan="1">Adipose tissue</td>
<td align="left" valign="top" rowspan="1" colspan="1">Adenylate cyclase activation; regulation of body weight</td>
</tr>
</tbody>
</table>
<table-wrap-foot><p><italic>STN, subthalamic nucleus; LTP, long-term potentiation; cAMP, cyclic adenosine monophosphate</italic>
.</p>
</table-wrap-foot>
</table-wrap>
</sec>
<sec><title>The locus coeruleus</title>
<p>The LC nucleus is present in all mammalian species and represents the main source of NA for the central nervous system (Mann, <xref ref-type="bibr" rid="B88">1983</xref>
; Aston-Jones, <xref ref-type="bibr" rid="B5">2004</xref>
). Synaptic inputs from several sources influence the activity of LC neurons. The LC NAergic system, via its widespread projections, modulates cortical, subcortical, and brainstem circuits. Due to the very small size of the LC, biochemical studies are unable to differentiate LC nucleus vs surrounding areas. A lot of retrograde and anterograde tract tracing studies over the years, that have been well recapitulated by Aston-Jones (<xref ref-type="bibr" rid="B5">2004</xref>
) and Benarroch (<xref ref-type="bibr" rid="B15">2009</xref>
), have demonstrated the numerous afferent and efferent connections of LC neurons. These reviews document that the orbitofrontal and anterior cingulate cortices provide the main source of glutamatergic afferent drive to the LC. LC modulates a variety of central functions through the release of NA into several brain areas including neocortex, hippocampus, thalamus, subthalamic nucleus, and substantia nigra. These projections are only sparse in striatum and spinal cord. Figure <xref ref-type="fig" rid="F1">1</xref>
summarizes the major afferent and efferent projections of the LC.</p>
<fig id="F1" position="float"><label>Figure 1</label>
<caption><p><bold>Afferent (red and purple) and efferent projections of LC neurons (blue)</bold>
. LC, locus coeruleus; NA, noradrenaline; Alpha2, Alpha2 receptor; GABA, γ-aminobutyrique acid; GABA A, GABA A receptor; 5-HT, serotonin; 5-HT1 and 5-HT2, serotonin receptor subtype 1 and 2; CRF, corticotropin releasing factor; STN, subthalamic nucleus; VTA, ventral tegmental area; SN, substantia nigra; NET, noradrenalinergic transporters; Red, excitatory input; Purple, inhibitory input.</p>
</caption>
<graphic xlink:href="fnsys-05-00031-g001"></graphic>
</fig>
<p>The biochemistry of NA neurons has relevance to PD. Because <sc>l</sc>
-Dopa, the metabolic precursor of DA, given to patients to enhance DA synthesis, is also a metabolic precursor of NA. In the normal condition, tyrosine hydroxylase (TH) catalyzes the conversion of the amino acid tyrosine to <sc>l</sc>
-Dopa. Both normally produced and administered <sc>l</sc>
-Dopa are catalyzed to DA by <sc>l</sc>
-aromatic amino acid decarboxylase (AADC). DA beta-hydroxylase (DBH) synthesizes NA from DA in the cytosol and either the vesicular monoamine transporter (VMAT) moves the NA into vesicles ready for exocytotic release or monoamine oxidase A degrades the NA. Once released into the extracellular space, reuptake of NA is performed by the plasmalemmal noradrenaline transporter (Rascol et al., <xref ref-type="bibr" rid="B118">2001</xref>
), while extracellular NA also limits its own release through the stimulation of auto-inhibitory α2 ARs (Figure <xref ref-type="fig" rid="F1">1</xref>
). Of note, as reported in the cortex (Tanda et al., <xref ref-type="bibr" rid="B140">1997</xref>
), NET can also transport extracellular DA inside NAergic neurons.</p>
<p>The LC NAergic system contributes to long-term synaptic plasticity, pain modulation, energy homeostasis and control of local blood flow (McCormick, <xref ref-type="bibr" rid="B97">1992</xref>
). LC neurons fire in two distinct modes, tonic and phasic (Aston-Jones and Cohen, <xref ref-type="bibr" rid="B6">2005a</xref>
,<xref ref-type="bibr" rid="B7">b</xref>
). Tonic activity is characterized by a sustained and highly regular pattern of discharge that is highest during wakefulness and decreases during slow-wave sleep. This tonic activity plays a central role in the sleep–waking cycle anticipating the fluctuations of electroencephalographic activity and promoting a state of vigilance. It is indeed well known that the stimulation of central NAergic receptors leads to changes in the state of vigilance. There is also a sustained increase in tonic discharge rate in response to environmental stimuli that elicit behavioral arousal and exploratory behavior. During focused attention and accurate task performance, LC neurons reduce their tonic firing to a moderate rate and respond phasically to task--relevant stimuli. The phasic bursts of LC activity are closely associated with highly accurate behavioral responses. Thus the LC nucleus has a major role in arousal, attention and stress response (Berridge and Waterhouse, <xref ref-type="bibr" rid="B19">2003</xref>
; Aston-Jones and Cohen, <xref ref-type="bibr" rid="B6">2005a</xref>
).</p>
<p>Alteration of the LC NAergic system has been implicated in many pathologies such as sleep and arousal disorders, attention deficit, hyperactivity disorder, post-traumatic stress disorder and psychiatric disorders, including anxiety, depression, schizophrenia, and mechanisms of opioid addiction (Benarroch, <xref ref-type="bibr" rid="B15">2009</xref>
). It constitutes a target for pharmacological treatment of these conditions (Aston-Jones, <xref ref-type="bibr" rid="B5">2004</xref>
; Rommelfanger and Weinshenker, <xref ref-type="bibr" rid="B124">2007</xref>
; Benarroch, <xref ref-type="bibr" rid="B15">2009</xref>
).</p>
</sec>
</sec>
<sec><title>The Locus Coeruleus Noradrenergic System in PD</title>
<p>Locus coeruleus is often severely affected in neurodegenerative diseases (Saper et al., <xref ref-type="bibr" rid="B128">1991</xref>
) and a growing number of anatomical and biochemical data has stressed this point in PD. In line with the drastic decrease in NAergic cell bodies (Chan-Palay and Asan, <xref ref-type="bibr" rid="B32">1989</xref>
), significant depletions (>80%) of NA concentration have also been reported in the PD brain (Taquet et al., <xref ref-type="bibr" rid="B141">1982</xref>
; Jenner et al., <xref ref-type="bibr" rid="B74">1983</xref>
; Gaspar et al., <xref ref-type="bibr" rid="B58">1991</xref>
). Consistently, Positron emission tomography (Dailly et al., <xref ref-type="bibr" rid="B38">2006</xref>
) studies have reported that [<sup>11</sup>
C]RTI-32, an <italic>in vivo</italic>
marker of both DA transporter (DAT) and NET binding, was reduced in several regions including those poorly innervated by DAergic fibers (Marie et al., <xref ref-type="bibr" rid="B90">1995</xref>
; Remy et al., <xref ref-type="bibr" rid="B121">2005</xref>
). It has also been shown that NAergic synapses change size and shape of the pre- and postsynaptic components, polymorphism of the synaptic vesicles and marked morphological alterations of the mitochondria (Chan-Palay and Asan, <xref ref-type="bibr" rid="B32">1989</xref>
; Baloyannis et al., <xref ref-type="bibr" rid="B11">2006</xref>
). Cash et al. (<xref ref-type="bibr" rid="B31">1984</xref>
, <xref ref-type="bibr" rid="B30">1986</xref>
) have reported an increase in the density of α1 and β1 ARs in synaptosomal and microsomal -fractions in the 6-hydroxydopamine (6-OHDA) rat model of PD (see below) as well as in the pre-frontal cortex of parkinsonian patients. The studies in animal models and PD patients suggest that the impairment of LC NAergic function could contribute to the motor and non-motor symptoms of PD.</p>
<sec><title>The locus coeruleus noradrenergic system in animal models of PD</title>
<p>A variety of models have been developed over the years with the increase in understanding of PD. Most, if not all, animal models have focused on DA depletion because PD symptoms typically occur in humans when approximately 70–80% of DA tissue content in the striatum has been lost (Bezard et al., <xref ref-type="bibr" rid="B22">2001</xref>
; McNamara and Durso, <xref ref-type="bibr" rid="B100">2006</xref>
). The impairment of the NAergic system, also typical of the human disease, has been neglected for several years to the point that most rat models of the disease, generated by administration of the catecholaminergic neurotoxin 6-OHDA, incorporate the concomitant protection of NAergic neurons with the NET blocker desipramine (see below). The reasons that have led to ignoring the role of NAergic neurons in the disease could be related to the demonstration that NAergic neurons are not directly responsible for the behavioral effects of <sc>l</sc>
-Dopa in animal models. Also, the striatum has been the main target of the anti-parkinsonian treatments, a brain region that is poorly innervated by NAergic fibers. Nonetheless, NAergic mechanisms may participate in the therapeutic outcome of <sc>l</sc>
-Dopa (Fox et al., <xref ref-type="bibr" rid="B52">2001</xref>
) and NA may act in brain regions that may profoundly impact on the control of motor behaviors, including the subthalamic nucleus (Belujon et al., <xref ref-type="bibr" rid="B14">2007</xref>
). The few data available regarding the various animal models of PD support a non-negligible role of NA in the aberrant motor output consequent to DA depletion.</p>
<p>Non-human primate models of the disease have been developed after the discovery of a specific neurotoxin 1-methyl-4-phenyl-l,2,3,6-tetrahydropyridine (MPTP) able to induce parkinsonism in humans (Langston and Ballard, <xref ref-type="bibr" rid="B83">1983</xref>
). MPTP has been shown to produce parkinsonian motor deficits in the non-human primate that are similar to PD (Langston and Ballard, <xref ref-type="bibr" rid="B82">1984</xref>
). This model has been essential in the understanding of the pathophysiology of PD (Fox and Brotchie, <xref ref-type="bibr" rid="B51">2010</xref>
) and the development of new therapeutic approaches, such as the lesion or high frequency stimulation of the subthalamic nucleus (Bergman et al., <xref ref-type="bibr" rid="B18">1990</xref>
; Benazzouz et al., <xref ref-type="bibr" rid="B17">1993</xref>
, <xref ref-type="bibr" rid="B16">1996</xref>
). MPTP-treated rhesus monkeys mimicked the DAergic cell degeneration in the SNc and profound striatal DA depletion. However, the inter-regional pattern of striatal DA loss typically encountered in the idiopathic PD, i.e., a significantly greater depletion of DA in the putamen compared to the caudate nucleus, is not reproduced in this model (Pifl et al., <xref ref-type="bibr" rid="B115">1991</xref>
). It was originally reported that MPTP did not cause LC cell death in non-human primates. However, it has become clear that MPTP also causes a distinct and often severe cell loss in the LC and/or NE depletion in terminal fields (Javitch et al., <xref ref-type="bibr" rid="B73">1984</xref>
; Mitchell et al., <xref ref-type="bibr" rid="B101">1985</xref>
; Di Paolo et al., <xref ref-type="bibr" rid="B44">1986</xref>
; Forno et al., <xref ref-type="bibr" rid="B50">1986</xref>
; Miyoshi et al., <xref ref-type="bibr" rid="B102">1988</xref>
; Pifl et al., <xref ref-type="bibr" rid="B115">1991</xref>
). MPTP-treated monkeys developed typical parkinsonian signs of bradykinesia, tremor, and hypokinesia. Behavioral symptoms of PD could involve the concomitant loss of DAergic and NAergic neurons, rather than DAergic neurons alone.</p>
<p>1-Methyl-4-phenyl-l,2,3,6-tetrahydropyridine has been also used in mice. MPTP-treated mice with 80% loss of DA do not exhibit profound motor impairments (German et al., <xref ref-type="bibr" rid="B59">1992</xref>
; Marien et al., <xref ref-type="bibr" rid="B91">2004</xref>
; Archer and Fredriksson, <xref ref-type="bibr" rid="B3">2006</xref>
). The fact that MPTP treatment in mice has little to no effect on LC neurons or NA tissue content may explain the lack of motor deficits. In support of a role of NA in motor symptoms in PD, DBH<sup>−/−</sup>
mice display motor impairments associated with a hypodopaminergic state. These mice synthesize normal amounts of DA, but, in the absence of NA, the release of DA seems to be decreased (Rommelfanger and Weinshenker, <xref ref-type="bibr" rid="B124">2007</xref>
). This is consistent with data reporting the excitatory influence exerted by NA on DAergic neuron function (see below interaction between DA and NA). One important note is that DBH<sup>−/−</sup>
mice are supplemented with NA agonists and NA itself during development as DBH is necessary for development (Thomas et al., <xref ref-type="bibr" rid="B143">1995</xref>
). Taken together, these data suggest that the behavioral symptoms of PD appear to be correlated with a concomitant loss of DA and NA.</p>
<p>The reserpinized rat model (Colpaert, <xref ref-type="bibr" rid="B36">1987</xref>
) and the VMAT KO mice (VMAT<sup>−/−</sup>
mice; Taylor et al., <xref ref-type="bibr" rid="B142">2009</xref>
) also support an interaction between DAergic and NAergic systems in PD motor symptoms. Reserpine blocks the VMAT, leading to a rapid decrease in the release of monoamines. The cardinal signs of the disease including tremor, rigidity, and hypokinesia are induced by reserpine in rats. The order of occurrence and time course of these signs appear to resemble the natural history of the human disease (Colpaert, <xref ref-type="bibr" rid="B36">1987</xref>
; Taylor et al., <xref ref-type="bibr" rid="B142">2009</xref>
). Surprisingly, drugs that increase postsynaptic ARs activation or NA availability, but not DA modulation, are effective in reducing parkinsonian signs in reserpinized rats (Colpaert, <xref ref-type="bibr" rid="B36">1987</xref>
). These observations led to the proposal that adrenergic mechanisms in the brain may play an important role in modifying motor and non-motor signs. As VMAT is impaired in both the reserpinized rats and the VMAT<sup>−/−</sup>
mice models, the involvement of serotonin (5-HT) in these mechanisms cannot be excluded because VMAT is also involved in the reuptake of serotonin. Reserpine treatments and VMAT<sup>−/−</sup>
mice do not only result in SNc DAergic and LC NAergic systems depletions, they also induce an almost total depletion of DA and NA from the other catecholaminergic nuclei as well as 5-HT originating from the raphe nuclei. In PD, it is estimated that 40–60% of 5-HT neurons degenerate in some cases (Kish, <xref ref-type="bibr" rid="B79">2003</xref>
; Kish et al., <xref ref-type="bibr" rid="B80">2008</xref>
; Politis et al., <xref ref-type="bibr" rid="B116">2010</xref>
).</p>
<p>The 6-OHDA rat is probably the most popular model of PD. Different 6-OHDA models of PD have been developed in which the toxin has been injected into different parts of the nigrostriatal pathway to cause DAergic cell loss in the SNc, resulting in DA depletion in the striatum (Deumens et al., <xref ref-type="bibr" rid="B42">2002</xref>
). 6-OHDA can be injected directly into the SNc, the medial forebrain bundle (MFB) or the striatum. The first two modes of injection are used to develop severe lesions of DAergic neurons corresponding to an advanced stage of the disease, while striatal injection of 6-OHDA is used to produce partial DA cell loss corresponding to the early stage of the disease (Kirik et al., <xref ref-type="bibr" rid="B78">1998</xref>
; Yuan et al., <xref ref-type="bibr" rid="B154">2005</xref>
; Breit et al., <xref ref-type="bibr" rid="B25">2007</xref>
). Such models exhibit some motor disabilities related to sensorimotor degradation though freezing, hypokinesia and tremor are not present. In addition, the non-motor symptoms are not evident (Amalric et al., <xref ref-type="bibr" rid="B1">1995</xref>
; Olsson et al., <xref ref-type="bibr" rid="B111">1995</xref>
; Branchi et al., <xref ref-type="bibr" rid="B24">2008</xref>
). It is noteworthy that 6-OHDA lesion of DAergic neurons causes LC NAergic neurons to be overactive with an irregular pattern of discharge (Wang et al., <xref ref-type="bibr" rid="B147">2009</xref>
), suggesting that their influence is magnified in DA-lesioned rats.</p>
<p>Noradrenaline depletion in the rodent by <italic>N</italic>
-(2-chloroethyl)-<italic>N</italic>
-ethyl-2-bromobenzylamine (DSP-4) is an approach commonly used to model human neuropsychiatric disorders in rodents. Even though the efficacy of DSP-4 in destroying NA fibers is region- and species-dependent (Dailly et al., <xref ref-type="bibr" rid="B38">2006</xref>
), convincing evidence indicates that DSP-4 is a neurotoxin that lesions NAergic terminals arising selectively from the LC (Fritschy and Grzanna, <xref ref-type="bibr" rid="B53">1989</xref>
; Grzanna et al., <xref ref-type="bibr" rid="B64">1989</xref>
; Fritschy and Grzanna, <xref ref-type="bibr" rid="B54">1991</xref>
). Concomitant to the data obtained in non-human primates and genetic mice models of PD (Pifl et al., <xref ref-type="bibr" rid="B115">1991</xref>
; Rommelfanger and Weinshenker, <xref ref-type="bibr" rid="B124">2007</xref>
), we have recently found that NA depletion alone induces severe motor deficits similar to those reported after 6-OHDA lesion (Delaville et al., <xref ref-type="bibr" rid="B40">2010</xref>
). In contrast to a 6-OHDA lesion (Deumens et al., <xref ref-type="bibr" rid="B42">2002</xref>
), the motor impairments consequent to NA depletion were not related to DAergic cell loss. Furthermore, the motor deficits reported in 6-OHDA-lesioned rats were not aggravated by the additional depletion of NA (Delaville et al., <xref ref-type="bibr" rid="B40">2010</xref>
). Another study has reported that denervation of LC NAergic terminals potentiated the 6-OHDA-induced partial DAergic neurodegeneration and akinesia only in rats treated with a D2 receptor antagonist, haloperidol (Srinivasan and Schmidt, <xref ref-type="bibr" rid="B134">2003</xref>
). Only a few studies have specifically addressed the non-motor symptoms of PD in animal models. Our recent data (Delaville et al., <xref ref-type="bibr" rid="B40">2010</xref>
) show that additional NA depletion in 6-OHDA-lesioned rats induced anxiety and fear behavior in the elevated plus maze, both being non-motor symptoms of PD. Recently, it has been reported that additional NA depletion impaired working memory in a manner similar to that observed after bilateral inactivation of LC suggesting that the NAergic system of the LC may play an important role in acquisition of spatial memory (Khakpour-Taleghani et al., <xref ref-type="bibr" rid="B77">2009</xref>
). Nevertheless, it has been reported that the deficits of spatial information processing in PD are solely a consequence of the striatal DAergic dysfunction (De Leonibus et al., <xref ref-type="bibr" rid="B41">2007</xref>
).</p>
<p>In conclusion, most animal models have focused on the motor symptoms related to the nigrostriatal DAergic system. A thorough examination of the data suggests that NAergic neuron dysfunction plays a non-negligible role in the motor and non-motor symptoms. The link between non-motor symptoms and the impairment of NAergic system has been also noted in humans.</p>
</sec>
<sec><title>Involvement of NA in PD symptoms</title>
<p>Although it is relatively common to describe a variety of significant biochemical alterations in PD patients, it is more difficult to demonstrate for each neurotransmitter a specific role in the pathophysiology of the disease. This point could be addressed by careful post-mortem studies which should correlate a specific biochemical pattern observed in a given patient with his detailed clinical history. PET imaging studies demonstrate that it is possible to assess <italic>in vivo</italic>
the neocortical monoamine terminal loss (including NA), and to elucidate its potential role in the complex cognitive and affective impairment in PD (Marie et al., <xref ref-type="bibr" rid="B90">1995</xref>
). This part of the review is focused on the most relevant studies investigating the role of NA depletion in specific motor and non-motor symptoms related to PD in human patients and associated with the above-mentioned animal models (Table <xref ref-type="table" rid="T2">2</xref>
).</p>
<table-wrap id="T2" position="float"><label>Table 2</label>
<caption><p><bold>Involvement of the LC in specific motor and non-motor symptoms of PD and their reference studies</bold>
.</p>
</caption>
<table frame="hsides" rules="groups"><thead><tr><td align="left" rowspan="1" colspan="1"></td>
<th align="left" rowspan="1" colspan="1">Symptoms</th>
<th align="left" rowspan="1" colspan="1">References</th>
</tr>
</thead>
<tbody><tr><td align="left" valign="top" rowspan="1" colspan="1">Motor symptoms</td>
<td align="left" valign="top" rowspan="1" colspan="1">Akinesia</td>
<td align="left" valign="top" rowspan="1" colspan="1">Hornykiewicz (<xref ref-type="bibr" rid="B70">1975</xref>
)<sup>H</sup>
, Narabayashi et al. (<xref ref-type="bibr" rid="B104">1991</xref>
)<sup>H</sup>
, Bezard et al. (<xref ref-type="bibr" rid="B21">1999</xref>
)<sup>M</sup>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" valign="top" rowspan="1" colspan="1">Freezing</td>
<td align="left" valign="top" rowspan="1" colspan="1">Tohgi et al. (<xref ref-type="bibr" rid="B146">1990</xref>
)<sup>H</sup>
, Mizuno et al., (<xref ref-type="bibr" rid="B103">1994</xref>
)<sup>H</sup>
, Sandyk (<xref ref-type="bibr" rid="B127">1996</xref>
)<sup>H</sup>
, Ringendahl and Sierla (<xref ref-type="bibr" rid="B123">1997</xref>
)<sup>H</sup>
, Devos et al. (<xref ref-type="bibr" rid="B43">2010</xref>
)<sup>H</sup>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" valign="top" rowspan="1" colspan="1">Locomotor activity</td>
<td align="left" valign="top" rowspan="1" colspan="1">Narabayashi et al. (<xref ref-type="bibr" rid="B104">1991</xref>
)<sup>H</sup>
, Nishi et al. (<xref ref-type="bibr" rid="B107">1991</xref>
)<sup>R</sup>
, Hill and Brotchie (<xref ref-type="bibr" rid="B68">1999</xref>
)<sup>R</sup>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" valign="top" rowspan="1" colspan="1">“On–off” phenomenon</td>
<td align="left" valign="top" rowspan="1" colspan="1">Sandyk (<xref ref-type="bibr" rid="B127">1996</xref>
)<sup>H</sup>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" valign="top" rowspan="1" colspan="1">Postural instability</td>
<td align="left" valign="top" rowspan="1" colspan="1">Narabayashi et al. (<xref ref-type="bibr" rid="B104">1991</xref>
)<sup>H</sup>
, Grimbergen et al. (<xref ref-type="bibr" rid="B62">2009</xref>
)<sup>H</sup>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" valign="top" rowspan="1" colspan="1">Tremor</td>
<td align="left" valign="top" rowspan="1" colspan="1">Colpaert (<xref ref-type="bibr" rid="B36">1987</xref>
)<sup>R</sup>
, Wilbur et al. (<xref ref-type="bibr" rid="B149">1988</xref>
)<sup>H</sup>
, Yamazaki et al. (<xref ref-type="bibr" rid="B152">1979</xref>
)<sup>R</sup>
</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1">Non-motor symptoms</td>
<td align="left" valign="top" rowspan="1" colspan="1">Anxiety</td>
<td align="left" valign="top" rowspan="1" colspan="1">Stein et al. (<xref ref-type="bibr" rid="B135">1990</xref>
)<sup>H</sup>
, Lauterbach et al. (<xref ref-type="bibr" rid="B85">2003</xref>
)<sup>H</sup>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" valign="top" rowspan="1" colspan="1">Attention and vigilance</td>
<td align="left" valign="top" rowspan="1" colspan="1">Stern et al. (<xref ref-type="bibr" rid="B136">1984</xref>
)<sup>H</sup>
, Mayeux et al. (<xref ref-type="bibr" rid="B95">1987</xref>
)<sup>H</sup>
, Bédard et al. (<xref ref-type="bibr" rid="B13">1998</xref>
)<sup>H</sup>
, Riekkinen et al. (<xref ref-type="bibr" rid="B122">1998</xref>
)<sup>H</sup>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" valign="top" rowspan="1" colspan="1">Dementia</td>
<td align="left" valign="top" rowspan="1" colspan="1">Mann and Yates (<xref ref-type="bibr" rid="B89">1983</xref>
)<sup>H</sup>
, Cash et al. (<xref ref-type="bibr" rid="B29">1987</xref>
)<sup>H</sup>
, Mayeux et al. (<xref ref-type="bibr" rid="B95">1987</xref>
)<sup>H</sup>
, Chan-Palay and Asan (<xref ref-type="bibr" rid="B32">1989</xref>
)<sup>H</sup>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" valign="top" rowspan="1" colspan="1">Depression</td>
<td align="left" valign="top" rowspan="1" colspan="1">Mayeux et al. (<xref ref-type="bibr" rid="B96">1986</xref>
)<sup>H</sup>
, Cummings (<xref ref-type="bibr" rid="B37">1992</xref>
)<sup>H</sup>
, Dooneief et al. (<xref ref-type="bibr" rid="B45">1992</xref>
)<sup>H</sup>
, Bader and Hell (<xref ref-type="bibr" rid="B10">1998</xref>
)<sup>H</sup>
, Kasper et al. (<xref ref-type="bibr" rid="B76">2000</xref>
)<sup>H</sup>
, Oertel et al. (<xref ref-type="bibr" rid="B108">2001</xref>
)<sup>H</sup>
, Schrag et al. (<xref ref-type="bibr" rid="B131">2001</xref>
)<sup>H</sup>
, Lemke (<xref ref-type="bibr" rid="B86">2002</xref>
)<sup>H</sup>
, Selikhova et al. (<xref ref-type="bibr" rid="B132">2002</xref>
)<sup>H</sup>
, Lemke et al. (<xref ref-type="bibr" rid="B87">2004</xref>
)<sup>H</sup>
, Yamamoto (<xref ref-type="bibr" rid="B150">2004</xref>
)<sup>H</sup>
, Remy et al. (<xref ref-type="bibr" rid="B121">2005</xref>
)<sup>H</sup>
</td>
</tr>
</tbody>
</table>
<table-wrap-foot><p><italic>H, human studies; M, Monkey studies; R, Rat studies</italic>
.</p>
</table-wrap-foot>
</table-wrap>
<list list-type="simple"><list-item><label>(a)</label>
<p>Motor symptoms</p>
<p>Parkinson's disease presents a wider spectrum of motor symptoms when both DA and NA deficiency are combined (Narabayashi et al., <xref ref-type="bibr" rid="B104">1991</xref>
). α2ARs agonism potentiates the anti-parkinsonian action of <sc>l</sc>
-Dopa treatment (Hill and Brotchie, <xref ref-type="bibr" rid="B68">1999</xref>
). It is also suggested that alpha-adrenergic mechanisms and in particular α2ARs, may be involved in reserpine-induced tremor and rigidity (Colpaert, <xref ref-type="bibr" rid="B36">1987</xref>
). In human, akathisia and pseudo-parkinsonian tremor are modulated by a NAergic pathway that projects from the LC to the limbic system (Wilbur et al., <xref ref-type="bibr" rid="B149">1988</xref>
); these symptoms are improved by an α2ARs agonist or a βARs antagonist (Wilbur et al., <xref ref-type="bibr" rid="B149">1988</xref>
). Several studies have also reported the involvement of the LC NA pathway in freezing (Mizuno et al., <xref ref-type="bibr" rid="B103">1994</xref>
; Sandyk, <xref ref-type="bibr" rid="B127">1996</xref>
; Ringendahl and Sierla, <xref ref-type="bibr" rid="B123">1997</xref>
; Devos et al., <xref ref-type="bibr" rid="B43">2010</xref>
), the “on–off” phenomenon (Sandyk, <xref ref-type="bibr" rid="B127">1996</xref>
), postural instability (Narabayashi et al., <xref ref-type="bibr" rid="B104">1991</xref>
), and akinesia (Hornykiewicz, <xref ref-type="bibr" rid="B70">1975</xref>
; Narabayashi et al., <xref ref-type="bibr" rid="B104">1991</xref>
).</p>
</list-item>
<list-item><label>(b)</label>
<p>Non-motor symptoms</p>
<p>Improvements in medication to treat the motor symptoms have highlighted the non-motor symptoms, which represent one of the main concerns of preclinical and clinical studies (Chaudhuri and Odin, <xref ref-type="bibr" rid="B33">2010</xref>
). The non-motor symptoms may appear many years before the onset of the motor complications in PD (Lemke et al., <xref ref-type="bibr" rid="B87">2004</xref>
). Whilst we focus on potential DAergic sources of mental dysfunction in PD, the potential role of NAergic systems should be kept in mind as well. Indeed, specific loss of DAergic and NAergic innervation of the limbic system is associated with cognitive and neurobehavioral problems, including dementia (Cash et al., <xref ref-type="bibr" rid="B29">1987</xref>
), depression (Cummings, <xref ref-type="bibr" rid="B37">1992</xref>
; Remy et al., <xref ref-type="bibr" rid="B121">2005</xref>
), anxiety (Stein et al., <xref ref-type="bibr" rid="B135">1990</xref>
; Lauterbach et al., <xref ref-type="bibr" rid="B85">2003</xref>
), and attention deficits (Riekkinen et al., <xref ref-type="bibr" rid="B122">1998</xref>
).</p>
</list-item>
</list>
<p>In a rat model of early stage PD, striatal DAergic degeneration and NAergic alterations in prefrontal cortex may have caused emotional reactivity and anxiety (Tadaiesky et al., <xref ref-type="bibr" rid="B138">2008</xref>
). These -findings are consistent with data showing that, in naive rats, NAergic function regulates the responsiveness to environmental cues and anxiety behavior (Lapiz et al., <xref ref-type="bibr" rid="B84">2001</xref>
). In humans, it is also thought that the enhanced anxiety found in elderly people may be related to the loss of DAergic and NAergic innervations (Gareri et al., <xref ref-type="bibr" rid="B56">2002</xref>
).</p>
<p>One of the most devastating non-motor symptoms in PD is depression (Cummings, <xref ref-type="bibr" rid="B37">1992</xref>
; Bader and Hell, <xref ref-type="bibr" rid="B10">1998</xref>
; Oertel et al., <xref ref-type="bibr" rid="B108">2001</xref>
; Schrag et al., <xref ref-type="bibr" rid="B131">2001</xref>
; Lemke, <xref ref-type="bibr" rid="B86">2002</xref>
; Yamamoto, <xref ref-type="bibr" rid="B150">2004</xref>
; Remy et al., <xref ref-type="bibr" rid="B121">2005</xref>
). The incidence of depression is currently high in PD, reaching a prevalence of 40% in some studies (Mayeux et al., <xref ref-type="bibr" rid="B96">1986</xref>
; Dooneief et al., <xref ref-type="bibr" rid="B45">1992</xref>
). The reason for the high frequency of depression in PD is poorly understood but, even if in some patients a dopamine agonist (pramipexole) can improve this symptom (Bxarone et al., <xref ref-type="bibr" rid="B26">2010</xref>
), the combined depletion of the three monoaminergic systems may be an explanation. In the unilateral rat model of PD, we have found that the DA depletion combined with NA depletion induced by DSP-4 and 5-HT depletion induced by the tryptophane hydroxylase inhibitor parachlorophenylalanine reduced the sucrose consumption and enhanced the time of immobility in the Porsolt test (Delaville et al., <xref ref-type="bibr" rid="B40">2010</xref>
). Importantly, only the combined depletions of all three monoamine systems resulted in a depressive-like behavior. It has been reported in humans that the binding of [<sup>11</sup>
C]RTI-32 in the LC and in several regions of the limbic system including the anterior cingulate cortex, the amygdala, and the ventral striatum was inversely correlated with the degree of apathy and the intensity of depression in the patients (Remy et al., <xref ref-type="bibr" rid="B121">2005</xref>
). [<sup>11</sup>
C]RTI-32 is a ligand displaying similar affinities to DAT and NET but with far lower affinity for the 5-HTergic transporter (Carroll et al., <xref ref-type="bibr" rid="B27">1995</xref>
). Thus, it seems that the DAergic and NAergic innervations are involved in PD depression and might specifically play a role in apathy, which is a major feature of depression. A histological study has shown that LC neuron morphology is more severely altered in PD with depression than in PD without depression (Chan-Palay and Asan, <xref ref-type="bibr" rid="B32">1989</xref>
).</p>
<p>It has also been shown that LC cell loss correlates significantly with performance on reaction time tasks and continuous performance tasks that measure attention and vigilance (Stern et al., <xref ref-type="bibr" rid="B136">1984</xref>
; Mayeux et al., <xref ref-type="bibr" rid="B95">1987</xref>
; Bedard et al., <xref ref-type="bibr" rid="B13">1998</xref>
; Riekkinen et al., <xref ref-type="bibr" rid="B122">1998</xref>
; McNamara and Durso, <xref ref-type="bibr" rid="B100">2006</xref>
). LC damage results in severe loss of cortical and limbic NAergic innervation with a 40–78% decrease in NA, its metabolites and related enzymes in PD. These changes are more marked in patients with dementia than in those without dementia (Cash et al., <xref ref-type="bibr" rid="B29">1987</xref>
; Mayeux et al., <xref ref-type="bibr" rid="B95">1987</xref>
).</p>
</sec>
</sec>
<sec><title>Evidence for the Interaction between NA and DA in PD</title>
<p>The concomitant loss of NA and DA could therefore promote aberrant motor and non-motor symptoms, suggesting that the two systems could interact in the brain. Only a few studies demonstrate the role of DA in NAergic modulation in PD. In addition to the increase in firing rate of LC NA neurons (Wang et al., <xref ref-type="bibr" rid="B147">2009</xref>
), an increase in the density of β ARs in the cerebral cortex, the forebrain, thalamic nuclei, the midbrain, the hippocampus, and the cerebellum has been reported in 6-OHDA rats with a selective DAergic neuron lesion (Johnson et al., <xref ref-type="bibr" rid="B75">1989</xref>
). In general, a decrease in DAergic neuron function seems to enhance NAergic system activity.</p>
<p>Although anatomical evidence for innervation of DA containing brain regions by NAergic fibers in the rat is scarce, functional studies suggest the existence of NAergic inputs that facilitate DAergic transmission (Jenner et al., <xref ref-type="bibr" rid="B74">1983</xref>
). Indeed, Ponzio et al. (<xref ref-type="bibr" rid="B117">1981</xref>
) demonstrated that NAergic nerve terminals originating from the LC may be involved in regulating the functional activity of the DAergic nerve terminals both in the cerebral cortex and the striatum. This regulation appears to be excitatory in nature and is present early in development. These data are confirmed by pharmacological studies showing that αlARs antagonism may reduce the sensitivity of the mesolimbic DAergic system to pharmacological or environmental challenge (Davis et al., <xref ref-type="bibr" rid="B39">1985</xref>
; Snoddy and Tessel, <xref ref-type="bibr" rid="B133">1985</xref>
; Auclair et al., <xref ref-type="bibr" rid="B8">2002</xref>
). Since most antipsychotic drugs exhibit both D2 receptor and α1ARs antagonist properties, they may alleviate psychosis not only through blockade of postsynaptic DAergic receptors, but also presynaptically on the mesolimbic DAergic system, through their α1ARs antagonistic action (Mathe et al., <xref ref-type="bibr" rid="B93">1996</xref>
). Conversely, stimulation of α2ARs and β1ARs elevates DA extracellular levels in the striatum by acting at sites downstream of the DAergic neurons themselves (Chopin et al., <xref ref-type="bibr" rid="B34">1999</xref>
; Hudson et al., <xref ref-type="bibr" rid="B71">1999</xref>
). More specifically, β1ARs and α2ARs regulate the phosphorylation of DARPP-32, a phosphoprotein regulated by DAergic transmission, in neostriatal neurons. Gi protein activation by α2ARs antagonizes Gs/PKA signaling mediated by D1 receptors and α2ARs in striatonigral and striatopallidal neurons respectively, thereby enhancing D2 receptor/Gi signaling in striatopallidal neurons (Hara et al., <xref ref-type="bibr" rid="B66">2010</xref>
). Reches and Meiner (<xref ref-type="bibr" rid="B120">1992</xref>
) did not report any change in striatal DA synthesis and release after lesions of the dorsal NA bundle (DNEB). It is therefore suggested that any possible effect of the LC on DA transmission in the striatum is not mediated by the DNEB.</p>
<p>In parallel, the LC NAergic system is thought to exert a neuroprotective influence on SNc DAergic neurons. The first hints that NA promotes DAergic neuron survival came from MPTP studies in non-human primates and mice (Mavridis et al., <xref ref-type="bibr" rid="B94">1991</xref>
; Fornai et al., <xref ref-type="bibr" rid="B49">1996</xref>
). These studies reported that the damage to nigrostriatal DAergic neurons induced by MPTP was potentiated by pre-treatment with DSP4. Rommelfanger et al. (<xref ref-type="bibr" rid="B125">2004</xref>
) subsequently showed that either pharmacological or genetic blockade of NET, which increases extracellular NA, also protects DAergic neurons from MPTP damage in mice. The mechanisms underlying the neuroprotective influence of NA are not clearly determined (Rommelfanger and Weinshenker, <xref ref-type="bibr" rid="B124">2007</xref>
).</p>
</sec>
<sec><title>Therapeutic Approaches Targeting the Naergic System</title>
<sec><title>Effects of <sc>l</sc>
-threo-dops on motor and non-motor symptoms</title>
<p>Treatment of PD has focused on supplementing DA levels indirectly through <sc>l</sc>
-Dopa administration or on stimulating directly DAergic receptors with DA agonists. Despite the success of these therapies, certain features of PD fail to respond to treatment and even worsen with DA replacement therapy. Among these incapacitating refractory symptoms are apathy, depression, memory loss, akathisia, postural instability, and sudden transient freezing. Clinical and experimental evidence suggests that NA deficiency may be responsible for some of these PD symptoms (see above).</p>
<p>The DA replacement therapy with <sc>l</sc>
-Dopa probably alters the activity of NAergic neurons. Indeed, <sc>l</sc>
-Dopa may enter NAergic neurons to be decarboxylated to DA. Nishi et al. (<xref ref-type="bibr" rid="B107">1991</xref>
) but not Hollister et al. (<xref ref-type="bibr" rid="B69">1979</xref>
), have suggested that central NAergic terminals play a significant role in the increase of locomotor activity induced by <sc>l</sc>
-Dopa administration in rats with striatal DA deficiency. Nevertheless, NAergic neurons do not release DA synthesized from <sc>l</sc>
-Dopa as it has been reported that the total destruction of 5-HTergic neurons abolished the releasing effect of <sc>l</sc>
-Dopa (Tanaka et al., <xref ref-type="bibr" rid="B139">1999</xref>
), even in brain regions receiving substantial amount of NAergic fibers (Navailles et al., <xref ref-type="bibr" rid="B105">2010a</xref>
,<xref ref-type="bibr" rid="B106">b</xref>
). On the other hand, NAergic neurons could participate in the clearance of extracellular DA. Indeed, because NET is able to transport DA, NAergic fibers could modify the pattern of <sc>l</sc>
-Dopa-induced DA release depending on the relative innervation of brain regions by NAergic neurons. Thus, in the striatum, it has been reported that desipramine enhanced <sc>l</sc>
-Dopa-induced DA release (Arai et al., <xref ref-type="bibr" rid="B2">2008</xref>
), suggesting that the clearance could be higher in brain regions more densely innervated. Finally, one could expect an increase in NA tissue content and/or an increase in NA release induced by <sc>l</sc>
-Dopa. The finding that the α2AR antagonist idazoxan is efficient in reducing the dyskinesia induced by <sc>l</sc>
-Dopa but not by the DA agonist apomorphine (Fox et al., <xref ref-type="bibr" rid="B52">2001</xref>
) in MPTP-treated monkeys supports a change in NAergic neuron function induced by <sc>l</sc>
-Dopa.</p>
<p><sc>l</sc>
-Threo-dihydroxyphenylserine (<sc>l</sc>
-threo-DOPS), an non-natural NAergic precursor, has been shown to be effective in relieving motor and non-motor symptoms of PD (Kuno, <xref ref-type="bibr" rid="B81">1997</xref>
). Indeed, in the rat, the duration of harmaline induced tremor was significantly reduced by intraventricular administration of <sc>l</sc>
-thero-DOPS (Yamazaki et al., <xref ref-type="bibr" rid="B152">1979</xref>
). In PD patients, Ogawa et al. (<xref ref-type="bibr" rid="B109">1984</xref>
, <xref ref-type="bibr" rid="B110">1985</xref>
) have shown that 10 days treatment with <sc>l</sc>
-threo-DOPS substantially improved patient's freezing episodes, rigidity, and dysarthria. Narabayashi et al. (<xref ref-type="bibr" rid="B104">1991</xref>
) have reported that treatment with <sc>l</sc>
-threo-DOPS, in combination with a peripheral AADC inhibitor, may have profound effects on freezing phenomena in patients with PD (Tohgi et al., <xref ref-type="bibr" rid="B146">1990</xref>
; Tohgi et al., <xref ref-type="bibr" rid="B145">1993</xref>
). Other aspects of akinesia also improved considerably in a majority of these patients (Yamamoto et al., <xref ref-type="bibr" rid="B151">1986</xref>
), although rigidity and tremor were barely affected (Jenner et al., <xref ref-type="bibr" rid="B74">1983</xref>
). When <sc>l</sc>
-threo-DOPS treatment was stopped, the freezing returned to almost the former level, even though the patients continued to receive <sc>l</sc>
-Dopa and benserazide. This could be explained by the fact that <sc>l</sc>
-Dopa measurably affects NA content in the cerebrospinal fluid compared to <sc>l</sc>
-threo-DOPS treatment (Maruyama et al., <xref ref-type="bibr" rid="B92">1996</xref>
). In addition to the improvement of motor symptoms, psychological symptoms have also been improved by <sc>l</sc>
-threo-DOPS (Suzuki et al., <xref ref-type="bibr" rid="B137">1984</xref>
; Azuma et al., <xref ref-type="bibr" rid="B9">1991</xref>
).</p>
</sec>
<sec><title>Effects of naergic receptor modulation on motor and non-motor symptoms</title>
<p>α2ARs are distributed widely within the basal ganglia, including the substantia nigra (Schapira, <xref ref-type="bibr" rid="B130">2005</xref>
). Mavridis et al. (<xref ref-type="bibr" rid="B94">1991</xref>
) have suggested that the activation of α1ARs, which results in an increase in NAergic tone, facilitates locomotor activity, and inversely, α2ARs activation, by decreasing NAergic tone, inhibits locomotor activity. In PD, hypoactivation of NAergic tone may be involved in the manifestation of tremor and rigidity. In the reserpine rat, yohimbine, an α2ARs antagonist blocked tremor and improved rigidity but not hypokinesia (Colpaert, <xref ref-type="bibr" rid="B36">1987</xref>
).</p>
<p>In the 6-OHDA rat and MPTP monkey models of PD, blockade of α2ARs by idazoxan improved motor disabilities (Bezard et al., <xref ref-type="bibr" rid="B21">1999</xref>
; Belujon et al., <xref ref-type="bibr" rid="B14">2007</xref>
) in a manner comparable to that induced by a minimal dose of <sc>l</sc>
-Dopa (Bezard et al., <xref ref-type="bibr" rid="B21">1999</xref>
). Although these findings provide support for the therapeutic potential of α2ARs in the treatment of PD, idazoxan as a monotherapy in PD patients did not display anti-parkinsonian actions (Henry et al., <xref ref-type="bibr" rid="B67">1999</xref>
; Rascol et al., <xref ref-type="bibr" rid="B118">2001</xref>
; Colosimo and Craus, <xref ref-type="bibr" rid="B35">2003</xref>
). However, co-administration of idazoxan with <sc>l</sc>
-Dopa can provide an anti-parkinsonian action lasting more than twice the duration obtained with <sc>l</sc>
-Dopa alone. Interestingly, the α2AR agonist clonidine and βARs blockers like propranolol are effective in treating akathisia and tardive dyskinesia (Wilbur et al., <xref ref-type="bibr" rid="B149">1988</xref>
). However, clonidine is more often used to treat attention deficit in PD. Attention accuracy was not affected by withdrawal of DAergic drugs in mild or severe PD patients. Clonidine retarded accuracy of performance in a difficult attention test in PD patients (Riekkinen et al., <xref ref-type="bibr" rid="B122">1998</xref>
). It seems that the NAergic system via α2AR may act differentially on the manifestation of motor and non-motor symptoms in PD. α2AR antagonism would lead to motor amelioration whereas α2ARs agonism would have non-motor benefits.</p>
<p>Non-motor symptoms are also improved by the use of selective α1AR agonists. For example, naphtoxazine may improve performance in some cognitive tests of “frontal functions,” including the Stroop and the odd-man-out tests, which have been previously found to be affected in PD (Bedard et al., <xref ref-type="bibr" rid="B13">1998</xref>
). This drug reduced the percentage of errors and restored the lateralization of N100 during the shifting reaction time task, suggesting that it may act on the processes underlying the shifting deficit in these patients (Bedard et al., <xref ref-type="bibr" rid="B13">1998</xref>
). NAergic compounds could also be efficient in depression in PD. Reboxetine, a specific NET inhibitor, significantly improved depression scores (Lemke, <xref ref-type="bibr" rid="B86">2002</xref>
). This agent did not significantly change parkinsonian motor symptoms or dosage of <sc>l</sc>
-Dopa. Reboxetine was effective and well tolerated in PD patients receiving 4 weeks of treatment of moderate-to-severe depression. Recently, however, the other NET inhibitor atomoxetine failed to reduce depression in PD patients (Weintraub et al., <xref ref-type="bibr" rid="B148">2010</xref>
). The use of selective NET inhibitors may be critically dependent on the status of NA neurons which, as mentioned above, can be severely damaged.</p>
<p>There are good theoretical and clinical reasons, including pharmacological specificity of effects and low incidence of side effects, to consider reboxetine, idazoxan, clonidine, or naphtoxazine for the treatment of different symptoms in different cases of PD. The efficacy of some of these drugs including the selective NET inhibitors would, however, be critically dependent on the status of LC NAergic fibers. Finally, the wide spectrum of pathophysiological conditions found in the human disease is still not directly addressed in animal models. The predictive efficacy of NAergic compounds in the treatment of non-motor symptoms in PD may require the development of better behavioral tests in animal models.</p>
</sec>
<sec><title>Effects of naergic agents on <sc>l</sc>
-dopa induced dyskinesia</title>
<p>The side effects associated with long-term <sc>l</sc>
-Dopa treatment today constitute an important cause of functional disability. Side effects such as abnormal involuntary movements and psychiatric disorders remain difficult to manage without causing an increase in parkinsonian immobility. Moreover, management of the phenomenon of the “off” period is limited by these same side effects. The causes of <sc>l</sc>
-Dopa-induced dyskinesia are unclear. It probably involves non-physiological pulsatile stimulation of DAergic receptors or non-physiological release of DA (e.g., from 5-HTergic nerve terminals) in the striatum (Tanaka et al., <xref ref-type="bibr" rid="B139">1999</xref>
; Carta et al., <xref ref-type="bibr" rid="B28">2007</xref>
; Navailles et al., <xref ref-type="bibr" rid="B106">2010b</xref>
). Treatments targeting non-DAergic neurotransmitter systems including glutamate, GABA, NA, acetylcholine, 5-HT, adenosine, and cholecystokinin have been studied (Colosimo and Craus, <xref ref-type="bibr" rid="B35">2003</xref>
). It has been recently proposed that lesion of the LC is correlated with the onset of <sc>l</sc>
-Dopa-induced dyskinesia (Fornai et al., <xref ref-type="bibr" rid="B48">2007</xref>
). In the 6-OHDA rat model, lesioned rats showed a sensitization–desensitization turning response, whereas in 6-OHDA rats with an additional NAergic degeneration induced by DSP-4, the turning activity was maximal throughout the test. Double-lesioned rats exhibited a lower percentage of dose failure episodes during treatment. NAergic denervation appears to be associated with prolonged long-term DAergic sensitization.</p>
<p>This type of response appears to be comparable to that reported in the clinical setting with intermittent <sc>l</sc>
-Dopa administration where no desensitization occurs once the abnormal response is established (Ruckert et al., <xref ref-type="bibr" rid="B126">1997</xref>
; Perez et al., <xref ref-type="bibr" rid="B112">2009a</xref>
,<xref ref-type="bibr" rid="B113">b</xref>
). Fulceri et al. (<xref ref-type="bibr" rid="B55">2007</xref>
) also demonstrated that unilateral damage to the NAergic system precedes the onset of dyskinesia and worsens the severity of <sc>l</sc>
-Dopa-induced contralateral abnormal involuntary movements in hemi-parkinsonian rats. Furthermore, increases in locomotor activity after <sc>l</sc>
-Dopa administration were markedly suppressed in DA and NA deficient groups. This may suggest that additional NAergic denervation selectively decreases the motor response to <sc>l</sc>
-Dopa treatment (Nishi et al., <xref ref-type="bibr" rid="B107">1991</xref>
; Mizuno et al., <xref ref-type="bibr" rid="B103">1994</xref>
; Perez et al., <xref ref-type="bibr" rid="B114">2007</xref>
).</p>
<p>In view of these results, NAergic modulation has been considered to decrease <sc>l</sc>
-Dopa side effects. In 6-OHDA rats, the α2AR antagonist atipamezole and the α2AR agonist dexmedetomidine increased and decreased contralateral circling evoked by <sc>l</sc>
-Dopa respectively. Atipamezole also prolonged the duration of action of <sc>l</sc>
-Dopa. The α1AR antagonist prazosin partially -antagonized the effect of <sc>l</sc>
-Dopa and had a strong inhibitory effect on the -atipamezole-induced potentiation of the <sc>l</sc>
-Dopa response (Haapalinna et al., <xref ref-type="bibr" rid="B65">2003</xref>
; Yavich et al., <xref ref-type="bibr" rid="B153">2003</xref>
). This suggests that atipamezole can modulate motor function indirectly, by stimulating the release of NA and directly, by blocking postsynaptic α2ARs in neurons other than NAergic ones.</p>
<p>In MPTP-treated monkeys, blockade of α2ARs by idazoxan in combination with <sc>l</sc>
-Dopa did not impair the anti-parkinsonian response but significantly reduced dyskinesias and delayed their onset, so that the “on” state without dyskinesias was prolonged. The antidyskinetic effect of idazoxan was maintained when repeatedly administered for 10 days and the locomotor response to <sc>l</sc>
-Dopa was significantly increased by chronic administration of idazoxan (Henry et al., <xref ref-type="bibr" rid="B67">1999</xref>
; Grondin et al., <xref ref-type="bibr" rid="B63">2000</xref>
; Fox et al., <xref ref-type="bibr" rid="B52">2001</xref>
). The same antidyskinetic effect has been shown with the α2ARs antagonists yohimbine, rauwolscine, and fipamezole (Gomez-Mancilla and Bedard, <xref ref-type="bibr" rid="B60">1993</xref>
; Henry et al., <xref ref-type="bibr" rid="B67">1999</xref>
; Grondin et al., <xref ref-type="bibr" rid="B63">2000</xref>
; Savola et al., <xref ref-type="bibr" rid="B129">2003</xref>
; Fox and Brotchie, <xref ref-type="bibr" rid="B51">2010</xref>
). In the case of idazoxan and fipamezole, an extension of the duration of action of levodopa was also observed. All these antagonists had no effect on their own on DA overflow (Yavich et al., <xref ref-type="bibr" rid="B153">2003</xref>
). On the other hand, the α2ARs agonist clonidine and the βARs antagonist propanolol markedly reduced the dyskinetic movements induced by <sc>l</sc>
-Dopa at the cost of a return to parkinsonism (Gomez-Mancilla and Bedard, <xref ref-type="bibr" rid="B60">1993</xref>
). Another study in the MPTP-lesioned primate has shown that idazoxan significantly reduced <sc>l</sc>
-Dopa-induced dyskinesia, suggesting that α2ARs stimulation may be involved in the generation of <sc>l</sc>
-Dopa-induced dyskinesia (Fox et al., <xref ref-type="bibr" rid="B52">2001</xref>
; Bara-Jimenez et al., <xref ref-type="bibr" rid="B12">2004</xref>
).</p>
<p>In humans, however, neither idazoxan nor fipamezole had any effect on duration of on time. These drugs have shown variable benefits in clinical trials (Rascol et al., <xref ref-type="bibr" rid="B119">1994</xref>
). The poor efficacy could be explained by the dose used in the different studies. In the MPTP primate model, a significant effect of idazoxan on dyskinesia was observed over a range of doses from 1 to 10 mg/kg whereas much lower doses were used in human studies (approximately 0.25–1.0 mg/kg). Similarly, the maximal efficacy of fipamezole in reducing <sc>l</sc>
-Dopa-induced dyskinesia in humans was low compared to that reported in the monkey. It is not clear whether the doses and routes employed of either drug might provide equivalent plasma or brain drug levels across the two species. Side effects with α2ARs antagonists used in human studies included hypertension, facial flushing, and headache which could be inherent to α2ARs blockade. These side effects were dose-dependent and doses higher than 20 mg were not well tolerated (Fox and Brotchie, <xref ref-type="bibr" rid="B51">2010</xref>
). However, other α2ARs antagonists could be developed. For example, it has been shown in rats that atipamezole had no effect on blood pressure (Haapalinna et al., <xref ref-type="bibr" rid="B65">2003</xref>
). Further studies are warranted to confirm the potential benefit of α2ARs antagonists in <sc>l</sc>
-Dopa-induced dyskinesia.</p>
</sec>
</sec>
<sec><title>Concluding Remarks</title>
<p>Studies in a variety of models and species indicate that NAergic cell loss in the LC could be a conditioning factor for the natural history of PD. LC NA exerts an excitatory drive on the nigrostriatal DAergic system. The use of therapeutic strategies leading to an increase in NA in the brain of PD patients may have a specific place in the treatment of the disease. Pharmacological modulation of the NAergic system, specifically with α2-AR antagonists, perhaps by inhibiting autoreceptor function, could be important in the treatment of different symptoms of PD and of <sc>l</sc>
-Dopa-induced dyskinesia.</p>
</sec>
<sec><title>Conflict of Interest Statement</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
</body>
<back><ack><p>Claire Delaville was supported by a fellowship from the Ministère de l'Education Nationale, de la Recherche et de la Technologie (MENRT). The University Bordeaux Segalen and the Centre National de la Recherche Scientifique (CNRS) funded this study. We wish to thank Dr. Martin Guthrie for English reading of the manuscript.</p>
</ack>
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